Variant #0000517282 (NC_000003.11:g.100570799_100570801dup, NC_000003.11(NM_015429.3):c.1160-6_1160-4dup (ABI3BP))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.100570799_100570801dup
DNA change (hg38) g.100851955_100851957dup
Published as ABI3BP(NM_015429.3):c.1160-6_1160-4dupTTT
ISCN -
DB-ID ABI3BP_000005
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABI3BP NM_015429.3 -/. - c.1160-6_1160-4dup r.spl? p.?


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